A47G (p.Ala47Gly) variant of IDH2 (P48735)
A47G (p.Ala47Gly) in IDH2 (P48735) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
A47G (p.Ala47Gly) variant details
- p.Ala47Gly
- ExAC rs201173543
- TOPMed rs201173543
- gnomAD rs201173543
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available